13278-12-1

Basic information

• Product Name: Cyclohexaneacetic acid, 4-tert-butyl-1-hydroxy-, tert-butyl ester
• Synonyms: Cyclohexaneacetic acid, 4-tert-butyl-1-hydroxy-, tert-butyl ester
• CAS NO: 13278-12-1
• Molecular Formula: C₁₆H₃₀O₃
• Molecular Weight: 270.41
• Mol File: 13278-12-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 336.3°Cat760mmHg
• Flash Point: 124.4°C
• Appearance: /
• Density: 0.982g/cm³
• Vapor Pressure: 7.82E-06mmHg at 25°C
• Refractive Index: 1.471
• CAS DataBase Reference: Cyclohexaneacetic acid, 4-tert-butyl-1-hydroxy-, tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexaneacetic acid, 4-tert-butyl-1-hydroxy-, tert-butyl ester(13278-12-1)
• EPA Substance Registry System: Cyclohexaneacetic acid, 4-tert-butyl-1-hydroxy-, tert-butyl ester(13278-12-1)

Safety Data

• Hazardous Substances Data: 13278-12-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H30O3/c1-14(2,3)12-7-9-16(18,10-8-12)11-13(17)19-15(4,5)6/h12,18H,7-11H2,1-6H3

Upstream product

• 5292-43-3 bromoacetic acid tert-butyl ester 
• 98-53-3 4-tercbutyl-cyclohexanone 
• 540-88-5 acetic acid tert-butyl ester 

Relevant articles and documents

Some uses of mischmetall in organic synthesis

Mischmetall, an alloy of the light lanthanides, has been used in a variety of organic reactions, either as a coreductant in samarium(II)-mediated reactions (Barbier and Grignard-type reactions, pinacolic coupling reactions) or as the promoter of Reformatsky-type reactions. It has been also employed as the starting material for easy syntheses of lanthanide trihalides, the reactivity of which has been explored in Imamoto and Luche-Fukuzawa reactions and in Mukaiyama aldol reactions.